Trial · NCT00188669
The Use of Pentoxifylline and Vitamin E in the Treatment of Chronic Breast Pain
NCT00188669, Phase 2, Terminated, University Health Network, Toronto
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Use of Pentoxifylline and Vitamin E in the Treatment of Chronic Breast Pain. Trials, record NCT00188669. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00188669
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Use of Pentoxifylline and Vitamin E in the Treatment of Chronic Breast Pain
- NCT number
- NCT00188669
- Status
- Terminated
- Phases
- Phase 2
- Enrollment
- 48 participants, estimated
- Lead sponsor
- University Health Network, Toronto
- Conditions
- Breast Neoplasms
- Interventions
- pentoxifylline, alpha-Tocopherol
- First posted
- 2005-09-16
- Last updated
- 2010-08-11
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | To assess improvement in breast pain with use of the interventional agents. | ||
| Primary | To assess improvement in patient function with the use of the interventional agents. | ||
| Secondary | To assess time to maximal improvement in pain, durability of response, quality of life changes during the study | ||
| Secondary | To qualitatively characterise presenting pain syndromes | ||
| Secondary | To examine techniques for objective assessment of breast edema and texture/fibrotic changes | ||
| Secondary | To investigate the feasibility of the use of high resolution (40MHz) ultrasound and whether changes can be measured |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00188669
GET https://conductscience.org/api/trials/v1/NCT00188669/registered